Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 133418 |
| ensemblid | ENSG00000170571.12 |
| hgncid | 30465 |
| symbol | EMB |
| name | embigin |
| refseq_nuc | NM_198449.3 |
| refseq_prot | NP_940851.1 |
| ensembl_nuc | ENST00000303221.10 |
| ensembl_prot | ENSP00000302289.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 50396192 |
| end | 50441288 |
| strand | - |
| ver | v1.2 |
| region | chr5:50396192-50441288 |
| region5000 | chr5:50391192-50446288 |
| regionname0 | EMB_chr5_50396192_50441288 |
| regionname5000 | EMB_chr5_50391192_50446288 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 340 | 88 | 58 | 140 | 14 | 38 | 104 | EMB_chr5_50391192_50446288 | EMB | MRALP others(322): Show |
chr5 | 50391192 | 50446288 |
| a0002 | 0/0 | 327 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | MRALP others(322): Show |
chr5 | 50391192 | 50446288 |
| a0003 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | MRALP others(322): Show |
chr5 | 50391192 | 50446288 |
| a0004 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | MRALP others(322): Show |
chr5 | 50391192 | 50446288 |
| a0005 | 0/0 | 327 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | MRALP others(322): Show |
chr5 | 50391192 | 50446288 |
| a0006 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | MANNF others(272): Show |
chr5 | 50391192 | 50446288 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 981 | 319 | 79 | 54 | 132 | 14 | 38 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0001c0002 | 0/0 | 981 | 18 | 9 | 2 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0001c0004 | 0/0 | 981 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0001c0007 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0002c0003 | 0/0 | 981 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0003c0008 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0004c0006 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0005c0009 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | ATGCG others(976): Show |
chr5 | 50391192 | 50446288 | ||
| a0006c0005 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | AAGCG others(976): Show |
chr5 | 50391192 | 50446288 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4202 | 128 | 20 | 25 | 56 | 8 | 18 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0002 | 0/0 | 4203 | 56 | 7 | 6 | 38 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0003 | 0/1 | 4203 | 36 | 6 | 3 | 21 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0004 | 0/0 | 4203 | 17 | 14 | 3 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0005 | 0/0 | 4203 | 24 | 14 | 4 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0006 | 0/0 | 4203 | 14 | 0 | 2 | 9 | 1 | 2 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0007 | 0/0 | 4203 | 12 | 0 | 6 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0008 | 0/0 | 4203 | 5 | 5 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0009 | 0/0 | 4203 | 4 | 4 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0010 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0012 | 0/0 | 4203 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0013 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0014 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0015 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0016 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0017 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0018 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0019 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0020 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0021 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0022 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0023 | 0/0 | 4202 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0024 | 0/0 | 4202 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0025 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0026 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0027 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0001t0028 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0002t0004 | 0/0 | 4203 | 15 | 6 | 2 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0002t0011 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0004t0004 | 0/0 | 4203 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0001c0007t0029 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0002c0003t0002 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0003c0008t0001 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0004c0006t0001 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4197): Show |
chr5 | 50391192 | 50446288 |
| a0005c0009t0002 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| a0006c0005t0006 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | CTTTT others(4198): Show |
chr5 | 50391192 | 50446288 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0016g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0017g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0018g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0019g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0021g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0022g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0023g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0024g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0025g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0026g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0027g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0001t0028g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0011g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0002t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0004t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0001c0007t0029g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0002c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0003c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0004c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0005c0009t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| a0006c0005t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00099 | hp2 | a0001 | c0001 | t0026 | g0133 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0090 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0166 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00544 | hp2 | a0001 | c0001 | t0014 | g0078 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00597 | hp1 | a0001 | c0001 | t0013 | g0080 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0227 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0160 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0036 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01167 | hp1 | a0001 | c0004 | t0004 | g0040 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01169 | hp1 | a0001 | c0004 | t0004 | g0040 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0266 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0057 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01257 | hp1 | a0001 | c0001 | t0028 | g0144 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01358 | hp1 | a0001 | c0001 | t0023 | g0238 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0124 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0230 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0039 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01975 | hp1 | a0001 | c0001 | t0025 | g0140 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01978 | hp1 | a0001 | c0001 | t0024 | g0200 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0234 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0091 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0267 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02647 | hp2 | a0004 | c0006 | t0001 | g0043 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0118 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02922 | hp2 | a0001 | c0001 | t0027 | g0069 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0063 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0261 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03098 | hp2 | a0001 | c0002 | t0011 | g0264 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0097 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0117 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0022 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03453 | hp2 | a0001 | c0002 | t0011 | g0039 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0123 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0151 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0158 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0022 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0159 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18612 | hp1 | a0001 | c0001 | t0014 | g0084 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18942 | hp1 | a0005 | c0009 | t0002 | g0074 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0270 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0192 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18961 | hp2 | a0001 | c0001 | t0013 | g0129 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18962 | hp2 | a0001 | c0001 | t0019 | g0224 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18965 | hp2 | a0001 | c0001 | t0016 | g0079 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18975 | hp2 | a0002 | c0003 | t0002 | g0088 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19003 | hp2 | a0001 | c0007 | t0029 | g0260 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19010 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19064 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19065 | hp1 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19077 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19088 | hp1 | a0006 | c0005 | t0006 | g0042 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0268 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ASW | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0092 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0229 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | GIH | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0010 | SAS | GIH | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02109 | hp1 | a0003 | c0008 | t0001 | g0241 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0058 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0062 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0219 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0263 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0269 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0132 | REF | REF | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0190 | REF | REF | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:50396192 | T | C | 1 | a0001 | 1 | HG03130.hp1 | splice_region_variant | LOW | c.*3081A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | chr5 | 50396192 | |||||||
| chr5:50403232 | C | T | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.823G>A | p.Val275Met | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 960/4202 | 823/984 | 275/327 | chr5 | 50403232 | |||
| chr5:50403375 | A | G | 1 | a0003 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.680T>C | p.Leu227Pro | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 817/4202 | 680/984 | 227/327 | chr5 | 50403375 | |||
| chr5:50410965 | C | A | 1 | a0003 | 1 | HG02109.hp1 | missense_variant&splice_region_variant | MODERATE | c.384G>T | p.Arg128Ser | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/9 | 521/4202 | 384/984 | 128/327 | chr5 | 50410965 | |||
| chr5:50411302 | G | C | 2 | a0002 a0005 |
3 | NA18942.hp1 NA18975.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.278C>G | p.Ser93Cys | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 3/9 | 415/4202 | 278/984 | 93/327 | chr5 | 50411302 | |||
| chr5:50441079 | C | T | 1 | a0004 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.73G>A | p.Ala25Thr | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 210/4202 | 73/984 | 25/327 | chr5 | 50441079 | |||
| chr5:50441150 | A | T | 1 | a0006 | 1 | NA19088.hp1 | start_lost | HIGH | c.2T>A | p.Met1? | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 139/4202 | 2/984 | 1/327 | chr5 | 50441150 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:50403200 | T | C | 1 | a0001c0004 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.855A>G | p.Thr285Thr | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 992/4202 | 855/984 | 285/327 | chr5 | 50403200 | |||
| chr5:50403449 | A | G | 1 | a0001c0007 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.606T>C | p.Pro202Pro | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 743/4202 | 606/984 | 202/327 | chr5 | 50403449 | |||
| chr5:50441053 | G | A | 1 | a0001c0002 | 18 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
synonymous_variant | LOW | c.99C>T | p.Asp33Asp | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 236/4202 | 99/984 | 33/327 | chr5 | 50441053 | |||
| chr5:50441092 | G | C | 1 | a0001c0004 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.60C>G | p.Leu20Leu | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 197/4202 | 60/984 | 20/327 | chr5 | 50441092 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:50396201 | A | G | 1 | a0001c0001t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 3072 | chr5 | 50396201 | ||||||
| chr5:50396209 | G | A | 1 | a0001c0001t0007 | 12 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3064C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 3064 | chr5 | 50396209 | ||||||
| chr5:50396483 | G | C | 1 | a0001c0001t0022 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2790C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2790 | chr5 | 50396483 | ||||||
| chr5:50396742 | C | T | 1 | a0001c0001t0016 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2531G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2531 | chr5 | 50396742 | ||||||
| chr5:50396761 | G | C | 2 | a0001c0001t0009 a0001c0001t0012 |
6 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2512C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2512 | chr5 | 50396761 | ||||||
| chr5:50396796 | G | GC | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2476_*2477insG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2476 | chr5 | 50396796 | ||||||
| chr5:50397168 | T | C | 1 | a0001c0001t0010 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2105A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2105 | chr5 | 50397168 | ||||||
| chr5:50397254 | C | T | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2019G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2019 | chr5 | 50397254 | ||||||
| chr5:50397297 | C | T | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1976G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1976 | chr5 | 50397297 | ||||||
| chr5:50397336 | A | G | 1 | a0001c0001t0019 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1937 | chr5 | 50397336 | ||||||
| chr5:50397624 | C | T | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1649G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1649 | chr5 | 50397624 | ||||||
| chr5:50397682 | A | C | 1 | a0001c0001t0018 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1591T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1591 | chr5 | 50397682 | ||||||
| chr5:50397718 | A | T | 1 | a0001c0007t0029 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1555 | chr5 | 50397718 | ||||||
| chr5:50397721 | G | C | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1552 | chr5 | 50397721 | ||||||
| chr5:50397780 | C | T | 1 | a0001c0002t0011 | 3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1493G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1493 | chr5 | 50397780 | ||||||
| chr5:50397934 | T | C | 1 | a0001c0001t0008 | 5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1339A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1339 | chr5 | 50397934 | ||||||
| chr5:50397956 | T | G | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1317 | chr5 | 50397956 | ||||||
| chr5:50398251 | T | C | 1 | a0001c0001t0024 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1022 | chr5 | 50398251 | ||||||
| chr5:50398309 | G | A | 1 | a0001c0001t0013 | 2 | HG00597.hp1 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*964C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 964 | chr5 | 50398309 | ||||||
| chr5:50398354 | C | T | 1 | a0001c0001t0028 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*919G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 919 | chr5 | 50398354 | ||||||
| chr5:50398547 | A | C | 1 | a0001c0001t0009 | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 726 | chr5 | 50398547 | ||||||
| chr5:50398564 | A | G | 1 | a0001c0001t0017 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 709 | chr5 | 50398564 | ||||||
| chr5:50398749 | T | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(12): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*524A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 524 | chr5 | 50398749 | ||||||
| chr5:50398799 | A | G | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 474 | chr5 | 50398799 | ||||||
| chr5:50398878 | T | A | 5 | a0001c0001t0004 a0001c0001t0014 a0001c0002t0004 others(2): Show |
39 | HG00544.hp2 HG01109.hp2 HG01167.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*395A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 395 | chr5 | 50398878 | ||||||
| chr5:50398879 | T | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 394 | chr5 | 50398879 | ||||||
| chr5:50399127 | G | A | 3 | a0001c0001t0006 a0001c0007t0029 a0006c0005t0006 |
16 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 146 | chr5 | 50399127 | ||||||
| chr5:50399214 | C | T | 9 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(6): Show |
82 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*59G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 59 | chr5 | 50399214 | ||||||
| chr5:50441245 | C | T | 1 | a0001c0001t0015 | 1 | NA19064.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 94 | chr5 | 50441245 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:50399316 | T | C | 1 | a0001c0001t0005g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-26A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399316 | |||||||
| chr5:50399492 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.967-202T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399492 | |||||||
| chr5:50399573 | A | C | 1 | a0001c0001t0001g0247 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.967-283T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399573 | |||||||
| chr5:50399602 | G | A | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.966+257C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399602 | |||||||
| chr5:50399772 | G | C | 1 | a0001c0001t0002g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.966+87C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399772 | |||||||
| chr5:50399927 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0154 |
3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.912-14T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399927 | |||||||
| chr5:50399934 | A | G | 1 | a0001c0001t0018g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.912-21T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399934 | |||||||
| chr5:50399951 | A | G | 1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.912-38T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399951 | |||||||
| chr5:50399974 | A | C | 18 | a0001c0001t0004g0099 a0001c0001t0010g0062 a0001c0001t0010g0063 others(15): Show |
22 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.912-61T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399974 | |||||||
| chr5:50400019 | G | A | 4 | a0001c0001t0008g0026 a0001c0001t0008g0176 a0001c0001t0008g0177 others(1): Show |
5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.912-106C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400019 | |||||||
| chr5:50400151 | C | T | 1 | a0001c0001t0028g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.912-238G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400151 | |||||||
| chr5:50400380 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0168 others(8): Show |
14 | HG01358.hp1 HG02293.hp1 NA18747.hp2 others(11): Show |
intron_variant | MODIFIER | c.912-467C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400380 | |||||||
| chr5:50400441 | G | T | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.912-528C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400441 | |||||||
| chr5:50400457 | T | C | 8 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(5): Show |
9 | HG01167.hp2 HG01261.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.912-544A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400457 | |||||||
| chr5:50400691 | T | C | 34 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(31): Show |
40 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.912-778A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400691 | |||||||
| chr5:50400745 | T | C | 18 | a0001c0001t0004g0099 a0001c0001t0010g0062 a0001c0001t0010g0063 others(15): Show |
22 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.912-832A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400745 | |||||||
| chr5:50400765 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.912-852C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400765 | |||||||
| chr5:50400811 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.912-898T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400811 | |||||||
| chr5:50400905 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.912-992G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400905 | |||||||
| chr5:50400974 | G | A | 8 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(5): Show |
9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.912-1061C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400974 | |||||||
| chr5:50401062 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.912-1149C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401062 | |||||||
| chr5:50401098 | A | G | 134 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(131): Show |
175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.912-1185T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401098 | |||||||
| chr5:50401306 | C | T | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.911+980G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401306 | |||||||
| chr5:50401402 | T | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0188 others(2): Show |
5 | HG03490.hp2 HG03704.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.911+884A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401402 | |||||||
| chr5:50401415 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.911+871G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401415 | |||||||
| chr5:50401488 | G | A | 134 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(131): Show |
175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.911+798C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401488 | |||||||
| chr5:50401495 | T | A | 1 | a0001c0001t0003g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.911+791A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401495 | |||||||
| chr5:50401581 | C | T | 2 | a0001c0001t0004g0044 a0001c0001t0004g0048 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.911+705G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401581 | |||||||
| chr5:50401594 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.911+692C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401594 | |||||||
| chr5:50401964 | C | T | 1 | a0001c0001t0009g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.911+322G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401964 | |||||||
| chr5:50402029 | C | T | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.911+257G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402029 | |||||||
| chr5:50402124 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.911+162G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402124 | |||||||
| chr5:50402173 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.911+113A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402173 | |||||||
| chr5:50402346 | G | A | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(159): Show |
207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.878-27C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402346 | |||||||
| chr5:50402392 | C | A | 1 | a0001c0001t0005g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.878-73G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402392 | |||||||
| chr5:50402754 | A | G | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.877+424T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402754 | |||||||
| chr5:50402777 | G | C | 9 | a0001c0001t0005g0032 a0001c0001t0005g0230 a0001c0001t0005g0231 others(6): Show |
11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.877+401C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402777 | |||||||
| chr5:50402789 | CT | C | 8 | a0001c0001t0005g0020 a0001c0001t0005g0070 a0001c0001t0005g0100 others(5): Show |
9 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.877+388delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402789 | |||||||
| chr5:50402876 | C | CA | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0239 others(11): Show |
14 | HG00597.hp1 HG00738.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.877+301dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | |||||||
| chr5:50402876 | C | CAA | 8 | a0001c0001t0002g0017 a0001c0001t0002g0111 a0001c0001t0004g0015 others(5): Show |
10 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.877+300_877+301dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | |||||||
| chr5:50402876 | CA | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0201 a0001c0001t0001g0208 others(16): Show |
20 | HG01167.hp2 HG01891.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.877+301delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | |||||||
| chr5:50402876 | CAA | C | 26 | a0001c0001t0005g0016 a0001c0001t0005g0020 a0001c0001t0005g0032 others(23): Show |
30 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.877+300_877+301del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | |||||||
| chr5:50403151 | AC | A | 3 | a0001c0001t0005g0230 a0001c0002t0011g0039 a0001c0002t0011g0264 |
4 | HG01433.hp2 HG01884.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+26delG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403151 | |||||||
| chr5:50403152 | C | A | 157 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(154): Show |
201 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.877+26G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403152 | |||||||
| chr5:50403159 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.877+19G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403159 | |||||||
| chr5:50403892 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.601-438G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403892 | |||||||
| chr5:50403973 | G | A | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-519C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403973 | |||||||
| chr5:50403997 | G | C | 4 | a0001c0001t0004g0099 a0001c0002t0004g0036 a0001c0002t0004g0261 others(1): Show |
5 | HG01109.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-543C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403997 | |||||||
| chr5:50404060 | G | C | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.601-606C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404060 | |||||||
| chr5:50404281 | G | A | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.601-827C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404281 | |||||||
| chr5:50404320 | A | T | 1 | a0001c0001t0003g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601-866T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404320 | |||||||
| chr5:50404569 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.601-1115G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404569 | |||||||
| chr5:50404627 | T | C | 26 | a0001c0001t0005g0016 a0001c0001t0005g0020 a0001c0001t0005g0032 others(23): Show |
30 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.600+1098A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404627 | |||||||
| chr5:50404735 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.600+990C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404735 | |||||||
| chr5:50404795 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+930T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404795 | |||||||
| chr5:50404872 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.600+853A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404872 | |||||||
| chr5:50404968 | T | C | 1 | a0001c0001t0003g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+757A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404968 | |||||||
| chr5:50404979 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600+746G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404979 | |||||||
| chr5:50405386 | T | TA | 3 | a0001c0001t0003g0130 a0001c0001t0003g0131 a0001c0001t0003g0141 |
3 | NA18961.hp1 NA18980.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.600+338dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405386 | |||||||
| chr5:50405486 | A | T | 1 | a0001c0001t0002g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.600+239T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405486 | |||||||
| chr5:50405685 | CTGT | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.600+37_600+39delAC others(1): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405685 | |||||||
| chr5:50405921 | A | G | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(159): Show |
207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.473-69T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50405921 | |||||||
| chr5:50406005 | G | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(5): Show |
10 | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.473-153C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406005 | |||||||
| chr5:50406142 | G | C | 7 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(4): Show |
8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-290C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406142 | |||||||
| chr5:50406226 | A | C | 1 | a0001c0001t0007g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.473-374T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406226 | |||||||
| chr5:50406236 | A | G | 1 | a0001c0001t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.473-384T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406236 | |||||||
| chr5:50406413 | A | T | 13 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(10): Show |
15 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.473-561T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406413 | |||||||
| chr5:50406645 | T | C | 1 | a0001c0001t0006g0024 | 2 | NA19006.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.473-793A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406645 | |||||||
| chr5:50406766 | C | T | 102 | a0001c0001t0001g0028 a0001c0001t0001g0194 a0001c0001t0002g0002 others(99): Show |
138 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.473-914G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406766 | |||||||
| chr5:50407046 | ACT | A | 5 | a0001c0001t0004g0054 a0001c0001t0004g0061 a0001c0001t0004g0094 others(2): Show |
5 | HG01167.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-1196_473-1195d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407046 | |||||||
| chr5:50407076 | C | T | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.473-1224G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407076 | |||||||
| chr5:50407325 | G | A | 1 | a0001c0002t0004g0263 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473-1473C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407325 | |||||||
| chr5:50407336 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.473-1484T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407336 | |||||||
| chr5:50407349 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.473-1497G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407349 | |||||||
| chr5:50407354 | C | CGCT | 13 | a0001c0001t0002g0017 a0001c0001t0002g0067 a0001c0001t0002g0071 others(10): Show |
14 | HG01243.hp2 HG02055.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.473-1505_473-1503d others(5): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407354 | |||||||
| chr5:50407632 | C | A | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.473-1780G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407632 | |||||||
| chr5:50407774 | G | C | 140 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(137): Show |
182 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.473-1922C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407774 | |||||||
| chr5:50407795 | C | G | 174 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(171): Show |
221 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.473-1943G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407795 | |||||||
| chr5:50408133 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.473-2281A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408133 | |||||||
| chr5:50408249 | TA | T | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.473-2398delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408249 | |||||||
| chr5:50408254 | C | T | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.473-2402G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408254 | |||||||
| chr5:50408347 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.473-2495G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408347 | |||||||
| chr5:50408461 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.472+2416C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408461 | |||||||
| chr5:50408490 | C | G | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.472+2387G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408490 | |||||||
| chr5:50409276 | C | T | 3 | a0001c0002t0004g0266 a0001c0002t0004g0267 a0001c0002t0004g0268 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.472+1601G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409276 | |||||||
| chr5:50409378 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.472+1499C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409378 | |||||||
| chr5:50409567 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+1310C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409567 | |||||||
| chr5:50409661 | G | T | 1 | a0001c0001t0025g0140 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.472+1216C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409661 | |||||||
| chr5:50409743 | T | C | 42 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(39): Show |
65 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.472+1134A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409743 | |||||||
| chr5:50409913 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02056.hp1 NA19055.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.472+964A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409913 | |||||||
| chr5:50409921 | A | G | 1 | a0002c0003t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.472+956T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409921 | |||||||
| chr5:50410001 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472+876T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410001 | |||||||
| chr5:50410080 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.472+797C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410080 | |||||||
| chr5:50410136 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.472+741T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410136 | |||||||
| chr5:50410151 | C | T | 2 | a0001c0001t0001g0197 a0002c0003t0002g0088 |
2 | NA18975.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.472+726G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410151 | |||||||
| chr5:50410155 | G | A | 1 | a0001c0001t0006g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.472+722C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410155 | |||||||
| chr5:50410449 | A | G | 3 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 |
3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.472+428T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410449 | |||||||
| chr5:50410493 | C | G | 5 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(2): Show |
6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+384G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410493 | |||||||
| chr5:50410558 | G | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.472+319C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410558 | |||||||
| chr5:50410643 | G | T | 1 | a0001c0001t0005g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472+234C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410643 | |||||||
| chr5:50410711 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472+166T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410711 | |||||||
| chr5:50410819 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0156 a0001c0001t0001g0243 others(1): Show |
6 | HG01192.hp2 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+58C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410819 | |||||||
| chr5:50410833 | T | C | 7 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(4): Show |
8 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+44A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410833 | |||||||
| chr5:50410855 | T | C | 17 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 others(14): Show |
21 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.472+22A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410855 | |||||||
| chr5:50411662 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.197-279C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411662 | |||||||
| chr5:50411667 | TACCCTAT others(3): Show |
T | 132 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(129): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.197-294_197-285del others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411667 | |||||||
| chr5:50411794 | T | G | 8 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(5): Show |
9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-411A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411794 | |||||||
| chr5:50411808 | G | A | 2 | a0001c0001t0005g0032 a0001c0001t0005g0230 |
3 | HG01433.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-425C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411808 | |||||||
| chr5:50412032 | A | G | 1 | a0001c0001t0005g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-649T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412032 | |||||||
| chr5:50412047 | T | G | 2 | a0001c0001t0003g0163 a0001c0001t0003g0164 |
2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.197-664A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412047 | |||||||
| chr5:50412189 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0208 |
2 | HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.197-806T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412189 | |||||||
| chr5:50412240 | C | CCA | 29 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(26): Show |
34 | HG01192.hp2 HG01433.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-859_197-858dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412240 | |||||||
| chr5:50412253 | C | CACACAG | 6 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
7 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-871_197-870ins others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412253 | |||||||
| chr5:50412255 | C | CACAG | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0005g0070 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.197-873_197-872ins others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412255 | |||||||
| chr5:50412257 | G | C | 11 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0005g0016 others(8): Show |
12 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-874C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | |||||||
| chr5:50412257 | G | GAC | 3 | a0001c0001t0001g0028 a0001c0001t0001g0194 a0001c0001t0001g0210 |
4 | HG01952.hp1 HG03017.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-876_197-875dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | |||||||
| chr5:50412257 | GAC | G | 132 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(129): Show |
173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.197-876_197-875del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | |||||||
| chr5:50412258 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0172 |
2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.197-875T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412258 | |||||||
| chr5:50412304 | C | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.197-921G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412304 | |||||||
| chr5:50412353 | A | G | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(54): Show |
82 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.197-970T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412353 | |||||||
| chr5:50412396 | A | G | 27 | a0001c0001t0004g0099 a0001c0001t0005g0016 a0001c0001t0005g0020 others(24): Show |
31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-1013T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412396 | |||||||
| chr5:50412514 | C | A | 1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197-1131G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412514 | |||||||
| chr5:50412577 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.197-1194G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412577 | |||||||
| chr5:50412624 | C | T | 33 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
39 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.197-1241G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412624 | |||||||
| chr5:50412662 | AC | A | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.197-1280delG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412662 | |||||||
| chr5:50412696 | T | C | 4 | a0001c0001t0009g0056 a0001c0001t0009g0059 a0001c0001t0009g0076 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1313A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412696 | |||||||
| chr5:50412701 | C | T | 3 | a0001c0002t0004g0266 a0001c0002t0004g0267 a0001c0002t0004g0268 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.197-1318G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412701 | |||||||
| chr5:50412730 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.197-1347C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412730 | |||||||
| chr5:50412883 | C | CT | 30 | a0001c0001t0001g0167 a0001c0001t0001g0237 a0001c0001t0002g0086 others(27): Show |
34 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-1501dupA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412883 | |||||||
| chr5:50412917 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1534A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412917 | |||||||
| chr5:50412918 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1535C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412918 | |||||||
| chr5:50412919 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1536C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412919 | |||||||
| chr5:50412939 | TAA | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-1558_197-1557d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412939 | |||||||
| chr5:50413049 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197-1666G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413049 | |||||||
| chr5:50413061 | C | G | 6 | a0001c0001t0009g0056 a0001c0001t0009g0059 a0001c0001t0009g0076 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-1678G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413061 | |||||||
| chr5:50413207 | A | T | 1 | a0001c0001t0004g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.197-1824T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413207 | |||||||
| chr5:50413215 | G | A | 8 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(5): Show |
9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-1832C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413215 | |||||||
| chr5:50413234 | T | C | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.197-1851A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413234 | |||||||
| chr5:50413269 | T | C | 6 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(3): Show |
7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1886A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413269 | |||||||
| chr5:50413461 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.197-2078A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413461 | |||||||
| chr5:50413584 | C | CT | 7 | a0001c0001t0002g0092 a0001c0001t0003g0014 a0001c0001t0004g0066 others(4): Show |
8 | HG00597.hp1 HG01346.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-2202dupA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413584 | |||||||
| chr5:50413616 | C | A | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-2233G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413616 | |||||||
| chr5:50413721 | G | A | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.197-2338C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413721 | |||||||
| chr5:50413880 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(264): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.197-2497G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413880 | |||||||
| chr5:50413914 | G | A | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0006c0005t0006g0042 |
3 | NA18945.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.197-2531C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413914 | |||||||
| chr5:50413918 | G | A | 1 | a0001c0001t0014g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.197-2535C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413918 | |||||||
| chr5:50413940 | C | A | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.197-2557G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413940 | |||||||
| chr5:50414147 | C | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.197-2764G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414147 | |||||||
| chr5:50414387 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0195 |
4 | NA18747.hp2 NA18955.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-3004G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414387 | |||||||
| chr5:50414421 | C | T | 173 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(170): Show |
220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.197-3038G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414421 | |||||||
| chr5:50414451 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.197-3068C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414451 | |||||||
| chr5:50414491 | C | T | 6 | a0001c0002t0004g0037 a0001c0002t0004g0038 a0001c0002t0004g0262 others(3): Show |
8 | NA18944.hp1 NA18977.hp1 NA18991.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-3108G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414491 | |||||||
| chr5:50414528 | C | CA | 56 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0119 others(53): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.197-3146dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | |||||||
| chr5:50414528 | C | CAA | 5 | a0001c0001t0001g0098 a0001c0001t0001g0202 a0001c0001t0002g0019 others(2): Show |
6 | HG01891.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-3147_197-3146d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | |||||||
| chr5:50414528 | CA | C | 24 | a0001c0001t0001g0169 a0001c0001t0001g0197 a0001c0001t0001g0221 others(21): Show |
25 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-3146delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | |||||||
| chr5:50414528 | CAA | C | 71 | a0001c0001t0002g0018 a0001c0001t0002g0105 a0001c0001t0003g0005 others(68): Show |
89 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.197-3147_197-3146d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | |||||||
| chr5:50414787 | C | T | 5 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(2): Show |
6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-3404G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414787 | |||||||
| chr5:50414803 | C | G | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0006c0005t0006g0042 |
3 | NA18945.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.197-3420G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414803 | |||||||
| chr5:50414876 | T | G | 42 | a0001c0001t0002g0105 a0001c0001t0003g0005 a0001c0001t0003g0025 others(39): Show |
51 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-3493A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414876 | |||||||
| chr5:50414955 | T | A | 1 | a0001c0001t0003g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.197-3572A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414955 | |||||||
| chr5:50415035 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-3652C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415035 | |||||||
| chr5:50415056 | C | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-3673G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415056 | |||||||
| chr5:50415061 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.197-3678T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415061 | |||||||
| chr5:50415151 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.197-3768T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415151 | |||||||
| chr5:50415165 | A | G | 2 | a0001c0002t0004g0266 a0001c0002t0004g0267 |
2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.197-3782T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415165 | |||||||
| chr5:50415180 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.197-3797C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415180 | |||||||
| chr5:50415305 | T | C | 1 | a0001c0001t0016g0079 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.197-3922A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415305 | |||||||
| chr5:50415319 | A | C | 1 | a0001c0001t0016g0079 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.197-3936T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415319 | |||||||
| chr5:50415453 | C | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-4070G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415453 | |||||||
| chr5:50415726 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.197-4343A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415726 | |||||||
| chr5:50415727 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.197-4344C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415727 | |||||||
| chr5:50415806 | T | C | 1 | a0001c0001t0028g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.197-4423A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415806 | |||||||
| chr5:50416184 | C | G | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.197-4801G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416184 | |||||||
| chr5:50416427 | T | G | 1 | a0001c0002t0004g0038 | 2 | NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.197-5044A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416427 | |||||||
| chr5:50416652 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.197-5269A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416652 | |||||||
| chr5:50416720 | G | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-5337C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416720 | |||||||
| chr5:50416792 | G | A | 1 | a0001c0001t0003g0014 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.197-5409C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416792 | |||||||
| chr5:50416820 | G | T | 1 | a0001c0002t0004g0262 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.197-5437C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416820 | |||||||
| chr5:50417003 | G | A | 1 | a0001c0001t0005g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-5620C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417003 | |||||||
| chr5:50417164 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.197-5781A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417164 | |||||||
| chr5:50417335 | T | C | 1 | a0001c0001t0002g0086 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.197-5952A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417335 | |||||||
| chr5:50417438 | T | C | 1 | a0001c0001t0004g0047 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.197-6055A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417438 | |||||||
| chr5:50417517 | CAATGTGA others(27): Show |
C | 1 | a0001c0001t0002g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.197-6168_197-6135d others(36): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417517 | |||||||
| chr5:50417695 | C | G | 3 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0112 |
3 | HG02615.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197-6312G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417695 | |||||||
| chr5:50417763 | T | C | 28 | a0001c0001t0001g0119 a0001c0001t0004g0015 a0001c0001t0004g0044 others(25): Show |
33 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.197-6380A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417763 | |||||||
| chr5:50417883 | A | G | 2 | a0001c0001t0005g0032 a0001c0001t0005g0230 |
3 | HG01433.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-6500T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417883 | |||||||
| chr5:50417991 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0154 |
3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-6608T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417991 | |||||||
| chr5:50418289 | C | G | 1 | a0001c0001t0027g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-6906G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418289 | |||||||
| chr5:50418349 | C | T | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.197-6966G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418349 | |||||||
| chr5:50418388 | C | T | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.197-7005G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418388 | |||||||
| chr5:50418557 | T | C | 27 | a0001c0001t0004g0099 a0001c0001t0005g0016 a0001c0001t0005g0020 others(24): Show |
31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-7174A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418557 | |||||||
| chr5:50418596 | T | C | 1 | a0001c0001t0003g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.197-7213A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418596 | |||||||
| chr5:50418601 | C | T | 2 | a0001c0001t0026g0133 a0001c0007t0029g0260 |
2 | HG00099.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.197-7218G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418601 | |||||||
| chr5:50418636 | G | A | 4 | a0001c0001t0009g0056 a0001c0001t0009g0059 a0001c0001t0009g0076 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7253C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418636 | |||||||
| chr5:50418929 | T | C | 1 | a0001c0001t0002g0017 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.197-7546A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418929 | |||||||
| chr5:50418992 | T | C | 1 | a0001c0001t0005g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-7609A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418992 | |||||||
| chr5:50419055 | C | T | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.197-7672G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419055 | |||||||
| chr5:50419059 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.197-7676A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419059 | |||||||
| chr5:50419091 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0094 a0001c0001t0004g0095 others(1): Show |
4 | HG02615.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-7708T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419091 | |||||||
| chr5:50419135 | G | C | 1 | a0004c0006t0001g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-7752C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419135 | |||||||
| chr5:50419146 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.197-7763G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419146 | |||||||
| chr5:50419343 | C | T | 1 | a0001c0001t0013g0129 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.197-7960G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419343 | |||||||
| chr5:50419422 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.197-8039G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419422 | |||||||
| chr5:50419532 | TACATACA others(5): Show |
T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0222 a0001c0001t0001g0235 others(3): Show |
8 | HG00673.hp2 HG02056.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-8161_197-8150d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419532 | |||||||
| chr5:50419536 | T | TACAC | 3 | a0001c0001t0002g0004 a0001c0001t0002g0019 a0001c0001t0003g0154 |
4 | HG02258.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8157_197-8154d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACAC | 4 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0087 others(1): Show |
5 | HG00609.hp2 HG00639.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8159_197-8154d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(1): Show |
41 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(38): Show |
54 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.197-8161_197-8154d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(3): Show |
18 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0018 others(15): Show |
19 | HG00642.hp1 HG01496.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-8163_197-8154d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(5): Show |
9 | a0001c0001t0002g0007 a0001c0001t0002g0082 a0001c0001t0003g0134 others(6): Show |
10 | HG00544.hp1 HG01361.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(7): Show |
11 | a0001c0001t0002g0007 a0001c0001t0002g0105 a0001c0001t0002g0110 others(8): Show |
11 | HG00438.hp1 HG01081.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(16): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(9): Show |
24 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0049 others(21): Show |
27 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(18): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(11): Show |
4 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0130 others(1): Show |
5 | HG02040.hp1 HG02080.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419536 | T | TACACACA others(13): Show |
2 | a0001c0001t0003g0005 a0001c0001t0003g0128 |
2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.197-8154_197-8153i others(22): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | |||||||
| chr5:50419548 | T | C | 104 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.197-8165A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | |||||||
| chr5:50419548 | T | TACACAC | 3 | a0001c0001t0005g0232 a0001c0001t0008g0176 a0001c0001t0008g0234 |
3 | HG02055.hp1 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.197-8171_197-8166d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | |||||||
| chr5:50419548 | T | TACACACA others(1): Show |
15 | a0001c0001t0004g0015 a0001c0001t0004g0099 a0001c0001t0005g0020 others(12): Show |
19 | HG01192.hp1 HG01433.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-8173_197-8166d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | |||||||
| chr5:50419548 | T | TACACACA others(3): Show |
34 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0046 others(31): Show |
39 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.197-8175_197-8166d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | |||||||
| chr5:50419548 | T | TACACACA others(5): Show |
3 | a0001c0001t0004g0055 a0001c0001t0004g0126 a0001c0004t0004g0040 |
4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8177_197-8166d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | |||||||
| chr5:50419570 | C | CACACACA others(5): Show |
1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.197-8188_197-8187i others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419570 | |||||||
| chr5:50419629 | T | C | 27 | a0001c0001t0004g0099 a0001c0001t0005g0016 a0001c0001t0005g0020 others(24): Show |
31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-8246A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419629 | |||||||
| chr5:50419751 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197-8368A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419751 | |||||||
| chr5:50419810 | A | C | 1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+8334T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419810 | |||||||
| chr5:50419945 | C | T | 2 | a0001c0002t0011g0039 a0001c0002t0011g0264 |
3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.196+8199G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419945 | |||||||
| chr5:50419968 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | HG01515.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.196+8176C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419968 | |||||||
| chr5:50420033 | AG | A | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.196+8110delC | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420033 | |||||||
| chr5:50420073 | T | C | 1 | a0001c0001t0005g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+8071A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420073 | |||||||
| chr5:50420076 | T | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.196+8068A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420076 | |||||||
| chr5:50420213 | C | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.196+7931G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420213 | |||||||
| chr5:50420249 | A | T | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+7895T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420249 | |||||||
| chr5:50420360 | T | C | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196+7784A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420360 | |||||||
| chr5:50420445 | T | G | 1 | a0001c0001t0006g0149 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.196+7699A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420445 | |||||||
| chr5:50420626 | T | G | 3 | a0001c0002t0004g0266 a0001c0002t0004g0267 a0001c0002t0004g0268 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+7518A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420626 | |||||||
| chr5:50420667 | C | T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0049 others(26): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+7477G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420667 | |||||||
| chr5:50420668 | G | T | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+7476C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420668 | |||||||
| chr5:50420748 | G | A | 1 | a0001c0001t0012g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196+7396C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420748 | |||||||
| chr5:50420798 | T | G | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+7346A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420798 | |||||||
| chr5:50421011 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0257 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.196+7133T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421011 | |||||||
| chr5:50421107 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196+7037G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421107 | |||||||
| chr5:50421237 | T | C | 27 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(24): Show |
32 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.196+6907A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421237 | |||||||
| chr5:50421288 | G | GA | 9 | a0001c0001t0005g0032 a0001c0001t0005g0230 a0001c0001t0005g0231 others(6): Show |
11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+6855dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421288 | |||||||
| chr5:50421315 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196+6829G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421315 | |||||||
| chr5:50421635 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.196+6509T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421635 | |||||||
| chr5:50421640 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196+6504G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421640 | |||||||
| chr5:50421749 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.196+6395G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421749 | |||||||
| chr5:50421910 | G | A | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6234C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421910 | |||||||
| chr5:50421919 | T | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6225A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421919 | |||||||
| chr5:50421945 | A | G | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.196+6199T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421945 | |||||||
| chr5:50421952 | G | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6192C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421952 | |||||||
| chr5:50422047 | A | T | 1 | a0001c0001t0006g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.196+6097T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422047 | |||||||
| chr5:50422203 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196+5941T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422203 | |||||||
| chr5:50422209 | C | A | 1 | a0001c0001t0002g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+5935G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422209 | |||||||
| chr5:50422243 | T | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.196+5901A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422243 | |||||||
| chr5:50422314 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.196+5830A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422314 | |||||||
| chr5:50422343 | A | G | 2 | a0001c0001t0003g0137 a0001c0001t0003g0138 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196+5801T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422343 | |||||||
| chr5:50422655 | G | T | 1 | a0001c0001t0004g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196+5489C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422655 | |||||||
| chr5:50422743 | C | T | 1 | a0001c0001t0005g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.196+5401G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422743 | |||||||
| chr5:50422825 | G | A | 5 | a0001c0001t0005g0032 a0001c0001t0005g0230 a0001c0001t0005g0231 others(2): Show |
6 | HG01433.hp2 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+5319C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422825 | |||||||
| chr5:50422863 | G | A | 1 | a0003c0008t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+5281C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422863 | |||||||
| chr5:50422949 | T | C | 1 | a0001c0001t0005g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196+5195A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422949 | |||||||
| chr5:50423100 | T | C | 1 | a0001c0001t0009g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.196+5044A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423100 | |||||||
| chr5:50423101 | TA | T | 10 | a0001c0001t0001g0168 a0001c0001t0001g0182 a0001c0001t0001g0183 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+5042delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423101 | |||||||
| chr5:50423200 | A | G | 1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+4944T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423200 | |||||||
| chr5:50423297 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+4847G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423297 | |||||||
| chr5:50423329 | G | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+4815C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423329 | |||||||
| chr5:50423331 | G | C | 1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+4813C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423331 | |||||||
| chr5:50423442 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.196+4702T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423442 | |||||||
| chr5:50423630 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+4514C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423630 | |||||||
| chr5:50423638 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.196+4506G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423638 | |||||||
| chr5:50423682 | T | C | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.196+4462A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423682 | |||||||
| chr5:50423772 | G | T | 42 | a0001c0001t0002g0105 a0001c0001t0003g0005 a0001c0001t0003g0025 others(39): Show |
51 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+4372C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423772 | |||||||
| chr5:50423775 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+4369C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423775 | |||||||
| chr5:50423788 | C | T | 41 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0049 others(38): Show |
50 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+4356G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423788 | |||||||
| chr5:50423846 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
7 | NA18942.hp2 NA19010.hp2 NA19057.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+4298T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423846 | |||||||
| chr5:50424357 | G | C | 100 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.196+3787C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424357 | |||||||
| chr5:50424527 | C | T | 1 | a0001c0001t0006g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.196+3617G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424527 | |||||||
| chr5:50424579 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.196+3565A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424579 | |||||||
| chr5:50425120 | T | C | 1 | a0001c0001t0004g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3024A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425120 | |||||||
| chr5:50425262 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0155 a0001c0001t0001g0167 |
3 | HG02559.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196+2882G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425262 | |||||||
| chr5:50425303 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+2841G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425303 | |||||||
| chr5:50425497 | G | GA | 27 | a0001c0001t0004g0099 a0001c0001t0005g0016 a0001c0001t0005g0020 others(24): Show |
31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.196+2646dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425497 | |||||||
| chr5:50425505 | C | CA | 5 | a0001c0001t0001g0028 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG01952.hp1 HG03017.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+2638dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425505 | |||||||
| chr5:50425512 | A | T | 8 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(5): Show |
9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+2632T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425512 | |||||||
| chr5:50425721 | G | A | 7 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(4): Show |
8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+2423C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425721 | |||||||
| chr5:50425735 | T | TTGCTCTG others(15): Show |
174 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(171): Show |
221 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.196+2408_196+2409i others(24): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425735 | |||||||
| chr5:50425739 | A | C | 9 | a0001c0001t0005g0032 a0001c0001t0005g0230 a0001c0001t0005g0231 others(6): Show |
11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+2405T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425739 | |||||||
| chr5:50425752 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.196+2392G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425752 | |||||||
| chr5:50425769 | C | T | 41 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0049 others(38): Show |
50 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+2375G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425769 | |||||||
| chr5:50425894 | G | A | 1 | a0005c0009t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.196+2250C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425894 | |||||||
| chr5:50426172 | A | G | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.196+1972T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426172 | |||||||
| chr5:50426240 | T | G | 1 | a0001c0001t0003g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+1904A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426240 | |||||||
| chr5:50426561 | A | C | 1 | a0001c0001t0014g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.196+1583T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426561 | |||||||
| chr5:50426607 | T | G | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.196+1537A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426607 | |||||||
| chr5:50426794 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.196+1350T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426794 | |||||||
| chr5:50426898 | G | GA | 10 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(7): Show |
12 | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+1245dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426898 | |||||||
| chr5:50426898 | GA | G | 121 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.196+1245delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426898 | |||||||
| chr5:50426920 | T | C | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+1224A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426920 | |||||||
| chr5:50426934 | C | T | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+1210G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426934 | |||||||
| chr5:50427045 | T | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+1099A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427045 | |||||||
| chr5:50427215 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196+929C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427215 | |||||||
| chr5:50427234 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(53): Show |
81 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.196+910G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427234 | |||||||
| chr5:50427489 | C | CATT | 50 | a0001c0001t0002g0105 a0001c0001t0003g0005 a0001c0001t0003g0025 others(47): Show |
60 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.196+652_196+654dup others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427489 | |||||||
| chr5:50427489 | CATT | C | 19 | a0001c0001t0004g0055 a0001c0001t0004g0066 a0001c0001t0010g0062 others(16): Show |
23 | HG01109.hp2 HG01192.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.196+652_196+654del others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427489 | |||||||
| chr5:50427700 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.196+444C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427700 | |||||||
| chr5:50428398 | T | C | 1 | a0001c0001t0005g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-171A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428398 | |||||||
| chr5:50428437 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.113-210G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428437 | |||||||
| chr5:50428615 | G | A | 17 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 others(14): Show |
21 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.113-388C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428615 | |||||||
| chr5:50428745 | G | T | 6 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(3): Show |
7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-518C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428745 | |||||||
| chr5:50428750 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0154 |
3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.113-523C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428750 | |||||||
| chr5:50428880 | A | ATTTATT | 6 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(3): Show |
7 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-659_113-654dup others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428880 | |||||||
| chr5:50428880 | A | ATTTATTT others(5): Show |
1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113-665_113-654dup others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428880 | |||||||
| chr5:50429075 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0196 |
2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.113-848A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429075 | |||||||
| chr5:50429487 | A | C | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-1260T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429487 | |||||||
| chr5:50429499 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(6): Show |
10 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-1272T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429499 | |||||||
| chr5:50429522 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.113-1295C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429522 | |||||||
| chr5:50429879 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.113-1652G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429879 | |||||||
| chr5:50429968 | T | TTC | 21 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(18): Show |
23 | HG00738.hp1 HG01192.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.113-1743_113-1742d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | T | TTCTC | 12 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0027 others(9): Show |
14 | HG00673.hp2 HG01243.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.113-1745_113-1742d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | T | TTCTCTC | 6 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0180 others(3): Show |
6 | HG01261.hp2 HG01433.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1747_113-1742d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTC | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0175 others(15): Show |
19 | HG00639.hp1 HG01358.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.113-1743_113-1742d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTC | T | 28 | a0001c0001t0001g0030 a0001c0001t0001g0173 a0001c0001t0001g0174 others(25): Show |
31 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.113-1745_113-1742d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTC | T | 59 | a0001c0001t0001g0035 a0001c0001t0001g0198 a0001c0001t0002g0105 others(56): Show |
73 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.113-1747_113-1742d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTCT others(1): Show |
T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0154 a0001c0001t0005g0233 |
4 | HG02486.hp1 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1749_113-1742d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTCT others(3): Show |
T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0199 a0001c0001t0002g0111 others(14): Show |
18 | HG00099.hp2 HG01069.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.113-1751_113-1742d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTCT others(5): Show |
T | 1 | a0001c0001t0002g0017 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.113-1753_113-1742d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTCT others(7): Show |
T | 53 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(50): Show |
77 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.113-1755_113-1742d others(16): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429968 | TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1759_113-1742d others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | |||||||
| chr5:50429970 | C | T | 1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113-1743G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429970 | |||||||
| chr5:50429972 | C | T | 7 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(4): Show |
8 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1745G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429972 | |||||||
| chr5:50429974 | C | T | 22 | a0001c0001t0004g0055 a0001c0001t0004g0066 a0001c0001t0004g0095 others(19): Show |
25 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.113-1747G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429974 | |||||||
| chr5:50429976 | C | T | 58 | a0001c0001t0002g0105 a0001c0001t0003g0005 a0001c0001t0003g0025 others(55): Show |
72 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.113-1749G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429976 | |||||||
| chr5:50429978 | C | T | 10 | a0001c0001t0003g0014 a0001c0001t0003g0154 a0001c0001t0005g0016 others(7): Show |
12 | HG00735.hp2 HG01074.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.113-1751G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429978 | |||||||
| chr5:50429980 | C | T | 13 | a0001c0001t0002g0111 a0001c0001t0003g0121 a0001c0001t0003g0127 others(10): Show |
14 | HG00099.hp2 HG01069.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-1753G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429980 | |||||||
| chr5:50429982 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.113-1755G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429982 | |||||||
| chr5:50429984 | C | T | 53 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(50): Show |
77 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.113-1757G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429984 | |||||||
| chr5:50429988 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1761G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429988 | |||||||
| chr5:50429997 | T | A | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113-1770A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429997 | |||||||
| chr5:50429999 | T | A | 18 | a0001c0001t0002g0111 a0001c0001t0004g0126 a0001c0001t0005g0102 others(15): Show |
21 | HG01109.hp2 HG01192.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.113-1772A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429999 | |||||||
| chr5:50430001 | T | A | 32 | a0001c0001t0002g0017 a0001c0001t0002g0111 a0001c0001t0003g0014 others(29): Show |
39 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-1774A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430001 | |||||||
| chr5:50430003 | T | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(139): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.113-1776A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430003 | |||||||
| chr5:50430005 | T | A | 154 | a0001c0001t0001g0242 a0001c0001t0002g0002 a0001c0001t0002g0003 others(151): Show |
198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.113-1778A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430005 | |||||||
| chr5:50430034 | T | C | 1 | a0001c0001t0006g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.113-1807A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430034 | |||||||
| chr5:50430069 | G | A | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.113-1842C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430069 | |||||||
| chr5:50430168 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0111 |
3 | HG02976.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.113-1941G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430168 | |||||||
| chr5:50430232 | T | C | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-2005A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430232 | |||||||
| chr5:50430310 | A | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(4): Show |
8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-2083T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430310 | |||||||
| chr5:50430406 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.113-2179G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430406 | |||||||
| chr5:50430521 | T | C | 134 | a0001c0001t0001g0210 a0001c0001t0002g0002 a0001c0001t0002g0003 others(131): Show |
175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-2294A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430521 | |||||||
| chr5:50430589 | TG | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.113-2363delC | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430589 | |||||||
| chr5:50430593 | T | C | 174 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(171): Show |
221 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.113-2366A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430593 | |||||||
| chr5:50430627 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0246 |
2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.113-2400C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430627 | |||||||
| chr5:50430668 | T | G | 1 | a0001c0001t0005g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-2441A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430668 | |||||||
| chr5:50430739 | T | C | 8 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(5): Show |
9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-2512A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430739 | |||||||
| chr5:50431146 | T | C | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113-2919A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431146 | |||||||
| chr5:50431463 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-3236A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431463 | |||||||
| chr5:50431475 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-3248G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431475 | |||||||
| chr5:50431586 | AAT | A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(5): Show |
8 | HG01978.hp1 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-3361_113-3360d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431586 | |||||||
| chr5:50431629 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-3402C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431629 | |||||||
| chr5:50431884 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113-3657T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431884 | |||||||
| chr5:50432029 | C | T | 1 | a0002c0003t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-3802G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432029 | |||||||
| chr5:50432180 | A | G | 1 | a0001c0001t0007g0021 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.113-3953T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432180 | |||||||
| chr5:50432334 | AT | A | 4 | a0001c0001t0008g0026 a0001c0001t0008g0176 a0001c0001t0008g0177 others(1): Show |
5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-4108delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432334 | |||||||
| chr5:50432346 | A | C | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-4119T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432346 | |||||||
| chr5:50432369 | C | A | 42 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(39): Show |
65 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4142G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432369 | |||||||
| chr5:50432562 | T | TTAAAATA others(13): Show |
2 | a0001c0002t0011g0039 a0001c0002t0011g0264 |
3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.113-4355_113-4336d others(22): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432562 | |||||||
| chr5:50432750 | T | TA | 60 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0116 others(57): Show |
74 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.113-4524dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | |||||||
| chr5:50432750 | T | TAA | 6 | a0001c0001t0001g0119 a0001c0001t0003g0125 a0001c0001t0003g0147 others(3): Show |
6 | HG02258.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-4525_113-4524d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | |||||||
| chr5:50432750 | TA | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0172 others(16): Show |
23 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.113-4524delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | |||||||
| chr5:50432772 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.113-4545G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432772 | |||||||
| chr5:50432906 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-4679C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432906 | |||||||
| chr5:50432927 | A | T | 9 | a0001c0001t0002g0122 a0001c0001t0007g0021 a0001c0001t0007g0022 others(6): Show |
11 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-4700T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432927 | |||||||
| chr5:50432929 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.113-4702A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432929 | |||||||
| chr5:50433002 | C | T | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-4775G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433002 | |||||||
| chr5:50433100 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.113-4873A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433100 | |||||||
| chr5:50433350 | A | AG | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.113-5124_113-5123i others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433350 | |||||||
| chr5:50433373 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(6): Show |
10 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-5146G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433373 | |||||||
| chr5:50433442 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113-5215C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433442 | |||||||
| chr5:50433600 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0030 others(18): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.113-5373A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433600 | |||||||
| chr5:50433855 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.113-5628T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433855 | |||||||
| chr5:50433882 | G | A | 1 | a0001c0001t0006g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.113-5655C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433882 | |||||||
| chr5:50433905 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113-5678A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433905 | |||||||
| chr5:50433971 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-5744G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433971 | |||||||
| chr5:50434057 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-5830A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434057 | |||||||
| chr5:50434260 | C | A | 5 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0100 others(2): Show |
6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-6033G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434260 | |||||||
| chr5:50434427 | T | C | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(159): Show |
207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.113-6200A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434427 | |||||||
| chr5:50434448 | C | T | 1 | a0002c0003t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-6221G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434448 | |||||||
| chr5:50434497 | G | T | 134 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(131): Show |
175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-6270C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434497 | |||||||
| chr5:50434509 | T | G | 1 | a0002c0003t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-6282A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434509 | |||||||
| chr5:50434594 | G | C | 134 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(131): Show |
175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-6367C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434594 | |||||||
| chr5:50434664 | G | A | 7 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(4): Show |
8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6376C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434664 | |||||||
| chr5:50434672 | T | C | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+6368A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434672 | |||||||
| chr5:50434768 | T | C | 1 | a0002c0003t0002g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.112+6272A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434768 | |||||||
| chr5:50435055 | A | T | 1 | a0001c0001t0006g0023 | 2 | HG02040.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.112+5985T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435055 | |||||||
| chr5:50435093 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112+5947G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435093 | |||||||
| chr5:50435097 | G | A | 7 | a0001c0001t0004g0054 a0001c0001t0004g0061 a0001c0001t0004g0066 others(4): Show |
8 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+5943C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435097 | |||||||
| chr5:50435175 | A | G | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.112+5865T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435175 | |||||||
| chr5:50435333 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.112+5707A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435333 | |||||||
| chr5:50435352 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+5688G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435352 | |||||||
| chr5:50435414 | C | A | 1 | a0001c0001t0004g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.112+5626G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435414 | |||||||
| chr5:50435423 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.112+5617C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435423 | |||||||
| chr5:50435606 | G | A | 9 | a0001c0001t0004g0099 a0001c0001t0005g0020 a0001c0001t0005g0070 others(6): Show |
10 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+5434C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435606 | |||||||
| chr5:50435617 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0092 |
3 | HG02258.hp2 HG03209.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.112+5423G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435617 | |||||||
| chr5:50435769 | T | C | 1 | a0001c0001t0009g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+5271A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435769 | |||||||
| chr5:50435816 | A | G | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112+5224T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435816 | |||||||
| chr5:50435821 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | NA18939.hp2 NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.112+5219A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435821 | |||||||
| chr5:50436005 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+5035C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436005 | |||||||
| chr5:50436299 | T | C | 1 | a0001c0001t0003g0014 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.112+4741A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436299 | |||||||
| chr5:50436379 | A | G | 14 | a0001c0002t0004g0036 a0001c0002t0004g0037 a0001c0002t0004g0038 others(11): Show |
18 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.112+4661T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436379 | |||||||
| chr5:50436837 | T | G | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.112+4203A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436837 | |||||||
| chr5:50436843 | G | A | 11 | a0001c0001t0006g0010 a0001c0001t0006g0023 a0001c0001t0006g0024 others(8): Show |
15 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+4197C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436843 | |||||||
| chr5:50436932 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.112+4108A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436932 | |||||||
| chr5:50436994 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+4046C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436994 | |||||||
| chr5:50437128 | G | A | 7 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(4): Show |
8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+3912C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437128 | |||||||
| chr5:50437152 | T | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+3888A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437152 | |||||||
| chr5:50437294 | G | A | 4 | a0001c0001t0004g0055 a0001c0001t0010g0062 a0001c0001t0010g0063 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+3746C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437294 | |||||||
| chr5:50437376 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.112+3664C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437376 | |||||||
| chr5:50437674 | T | TGTCA | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.112+3362_112+3365d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437674 | |||||||
| chr5:50437716 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.112+3324T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437716 | |||||||
| chr5:50437800 | C | T | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG02293.hp2 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.112+3240G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437800 | |||||||
| chr5:50437954 | T | A | 1 | a0001c0001t0002g0007 | 4 | NA19003.hp1 NA19011.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+3086A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437954 | |||||||
| chr5:50437982 | C | G | 2 | a0001c0001t0002g0065 a0001c0001t0003g0014 |
3 | HG02486.hp1 HG03130.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.112+3058G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437982 | |||||||
| chr5:50438312 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.112+2728C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438312 | |||||||
| chr5:50438380 | G | C | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+2660C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438380 | |||||||
| chr5:50438506 | C | T | 1 | a0001c0001t0027g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.112+2534G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438506 | |||||||
| chr5:50438513 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0022g0219 |
3 | HG02630.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.112+2527T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438513 | |||||||
| chr5:50438589 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.112+2451A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438589 | |||||||
| chr5:50438605 | T | C | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+2435A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438605 | |||||||
| chr5:50438631 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.112+2409T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438631 | |||||||
| chr5:50438668 | T | C | 1 | a0001c0001t0005g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+2372A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438668 | |||||||
| chr5:50438671 | C | G | 27 | a0001c0001t0004g0099 a0001c0001t0005g0016 a0001c0001t0005g0020 others(24): Show |
31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.112+2369G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438671 | |||||||
| chr5:50438736 | A | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0155 a0001c0001t0001g0167 |
3 | HG02559.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.112+2304T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438736 | |||||||
| chr5:50438766 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0092 |
3 | HG02258.hp2 HG03209.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.112+2274A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438766 | |||||||
| chr5:50438847 | C | A | 1 | a0001c0001t0004g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112+2193G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438847 | |||||||
| chr5:50438903 | CT | C | 6 | a0001c0001t0002g0093 a0001c0001t0003g0014 a0001c0001t0003g0154 others(3): Show |
7 | HG01192.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+2136delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438903 | |||||||
| chr5:50438957 | C | T | 3 | a0001c0001t0004g0099 a0001c0001t0005g0100 a0001c0001t0009g0056 |
3 | HG02109.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.112+2083G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438957 | |||||||
| chr5:50439252 | C | T | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.112+1788G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439252 | |||||||
| chr5:50439411 | G | A | 3 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0112 |
3 | HG02615.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.112+1629C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439411 | |||||||
| chr5:50439487 | AT | A | 107 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 others(104): Show |
139 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.112+1552delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439487 | |||||||
| chr5:50439487 | ATT | A | 61 | a0001c0001t0002g0096 a0001c0001t0002g0113 a0001c0001t0003g0005 others(58): Show |
74 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.112+1551_112+1552d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439487 | |||||||
| chr5:50439536 | G | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.112+1504C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439536 | |||||||
| chr5:50439676 | C | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.112+1364G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439676 | |||||||
| chr5:50439895 | G | T | 5 | a0001c0001t0004g0055 a0001c0001t0004g0066 a0001c0001t0010g0062 others(2): Show |
5 | HG01346.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1145C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439895 | |||||||
| chr5:50439973 | T | C | 1 | a0001c0004t0004g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.112+1067A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439973 | |||||||
| chr5:50440086 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+954G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440086 | |||||||
| chr5:50440113 | CAT | C | 3 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02056.hp1 NA19055.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.112+925_112+926del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440113 | |||||||
| chr5:50440185 | G | A | 3 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 |
3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.112+855C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440185 | |||||||
| chr5:50440308 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.112+732G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440308 | |||||||
| chr5:50440337 | C | G | 1 | a0001c0001t0004g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112+703G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440337 | |||||||
| chr5:50440417 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.112+623G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440417 | |||||||
| chr5:50440533 | C | CA | 22 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0033 others(19): Show |
31 | HG00597.hp2 HG01070.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.112+506dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | C | CAA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
7 | HG00558.hp2 HG00741.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+505_112+506dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0005g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+487_112+506dup others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CA | C | 13 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00140.hp2 HG00738.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+506delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAA | C | 13 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(10): Show |
14 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+505_112+506del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAA | C | 46 | a0001c0001t0001g0009 a0001c0001t0001g0116 a0001c0001t0001g0119 others(43): Show |
58 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.112+504_112+506del others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAAA | C | 30 | a0001c0001t0001g0098 a0001c0001t0002g0004 a0001c0001t0002g0105 others(27): Show |
39 | HG00438.hp2 HG00642.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.112+503_112+506del others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAAAA | C | 50 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(47): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.112+502_112+506del others(5): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAAAAA | C | 12 | a0001c0001t0002g0060 a0001c0001t0002g0065 a0001c0001t0004g0054 others(9): Show |
12 | HG01167.hp2 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+501_112+506del others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0005g0016 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
6 | HG00642.hp2 HG01074.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+499_112+506del others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440533 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0049 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.112+497_112+506del others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | |||||||
| chr5:50440561 | A | G | 6 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(3): Show |
7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+479T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440561 | |||||||
| chr5:50440608 | T | G | 1 | a0001c0001t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.112+432A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440608 | |||||||
| chr5:50440933 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.112+107A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440933 | |||||||
| chr5:50440957 | C | A | 1 | a0001c0001t0001g0259 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+83G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440957 | |||||||
| chr5:50440988 | G | T | 1 | a0001c0001t0003g0014 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.112+52C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440988 | |||||||
| chr5:50441018 | C | A | 1 | a0001c0007t0029g0260 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+22G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50441018 |